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Volumetric analysis of the posterior cranial fossa in a family with four generations of the Chiari malformation Type I

R. Shane Tubbs Department of Cell Biology, University of Alabama at Birmingham;
Division of Neurosurgery, Children's Hospital;

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 M.S., P.A.-C., Ph.D.
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Mark Hill University of Alabama at Birmingham School of Medicine, Birmingham, Alabama;

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 B.S.
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Marios Loukas Department of Anatomical Sciences, St. George's University, Grenada; and

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 M.D., Ph.D.
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Mohammadali M. Shoja Tuberculosis and Lung Disease Institute, Tabriz Medical University, Tabriz, Iran

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W. Jerry Oakes Division of Neurosurgery, Children's Hospital;

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Object

Many authors have concluded that the Chiari malformation Type I (CM-I) is due to a smaller than normal posterior cranial fossa. In order to establish this smaller geometry as the cause of hindbrain herniation in a family, the authors of this paper performed volumetric analysis in a family found to have this malformation documented in 4 generations.

Methods

Members from this family found to have a CM-I by imaging underwent volumetric analysis of their posterior cranial fossa using the Cavalieri method.

Results

No member of this family found to have CM-I on preoperative imaging had a posterior fossa that was significantly smaller than that of age-matched controls.

Conclusions

The results of this study demonstrate that not all patients with a CM-I will have a reduced posterior cranial fossa volume. Although the mechanism for the development of hindbrain herniation in this cohort is unknown, this manifestation can be seen in multiple generations of a familial aggregation with normal posterior fossa capacity.

Abbreviations used in this paper:

CM-I = Chiari malformation Type I; GH = growth hormone; MR = magnetic resonance.
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  • 1

    Atkinson JL, , Kokmen E, & Miller GM: Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation: case report. Neurosurgery 42:401404, 1998

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 2

    Badie B, , Mendoza D, & Batzdorf U: Posterior fossa volume and response to suboccipital decompression in patients with Chiari I malformation. Neurosurgery 37:214218, 1995

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3

    Boyles AL, , Enterline DS, , Hammock PH, , Siegel DG, , Slifer SH, & Mehltretter L, et al.: Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15. Am J Med Genet A 15:27762785, 2006

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 4

    Cavender RK, & Schmidt JH III: Tonsillar ectopia and Chiari malformations: monozygotic triplets. Case report. J Neurosurg 82:497500, 1995

  • 5

    Coria F, , Quintana F, , Rebollo M, , Combarros O, & Berciano J: Occipital dysplasia and Chiari type I deformity in a family. J Neurol Sci 62:147158, 1983

  • 6

    Fijisawa H, , Hasegawa M, , Kida S, & Yamashita J: A novel fibro-blast growth factor receptor 2 mutation in Crouzon syndrome associated with Chiari type I malformation and syringomyelia. J Neurosurg 97:396400, 2002

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 7

    Gripp KW, , Scott CI Jr, , Nicholson L, , Magram G, & Grissom LE: Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda. Skeletal Radiol 26:131133, 1997

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 8

    Herman MD, , Cheek WR, & Storrs BB: Two siblings with the Chiari I malformation. Pediatr Neurosurg 16:183184, 1991

  • 9

    Marin-Padilla M, & Marin-Padilla TM: Morphogenesis of experimentally induced Arnold–Chiari malformation. J Neurol Sci 50:2955, 1981

  • 10

    Milhorat TH, , Chou MW, , Trinidad EM, , Kula RW, , Mandell M, & Wolpert C, et al.: Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44:10051017, 1999

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 11

    Murphy RL, , Tubbs RS, , Grabb PA, & Oakes WJ: Chiari I malformation and idiopathic growth hormone deficiency in siblings. Childs Nerv Syst 22:632634, 2006

  • 12

    Nishikawa M, , Sakamoto H, , Hakuba A, , Yasui T, , Kitano S, & Nakanishi N, et al.: Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa. J Neurosurg 86:4047, 1997

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 13

    Paquis P, , Lonjon M, , Brunet M, , Lambert JC, & Grellier P: Chiari Type I malformation and syringomyelia in unrelated patients with blepharophimosis. Report of two cases. J Neurosurg 89:835838, 1998

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 14

    Schimmenti LA, , Shim HH, , Wirtschafter JD, , Panzarino VA, , Kashtan CE, & Kirkpatrick SJ, et al.: Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndrome. Hum Mutat 14:369376, 1999

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 15

    Sgouros S, , Kountouri M, & Natarajan K: Posterior fossa volume in children with Chiari malformation Type I. J Neurosurg 105:2 Suppl 101106, 2006

  • 16

    Speer MC, , Enterline DS, , Mehltretter L, , Hammock P, , Joseph J, & Dickerson M, et al.: Chiari type 1 malformation with or without syringomyelia: prevalence and genetics. J Gen Counsel 12:297311, 2003

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 17

    Speer MC, , George TM, , Enterline DS, , Franklin A, , Wolpert CM, & Milhorat TH: A genetic hypothesis for Chiari I malformation with or without syringomyelia. Neurosurg Focus 8:3 E12, 2000

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 18

    Stovner JL, & Sjaastad O: Segmental hyperhidrosis in two siblings with Chiari type I malformation. Eur Neurol 35:149155, 1995

  • 19

    Tubbs RS, , Bui CJ, , Rice WC, , Loukas M, , Naftel RP, & Holcombe MP, et al.: Critical analysis of the Chiari malformation Type I found in children with lipomyelomeningocele. J Neurosurg 106:3 Suppl 196200, 2007

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 20

    Tubbs RS, , Elton S, , Grabb P, , Dockery SE, , Bartolucci AA, & Oakes WJ: Analysis of the posterior fossa in children with the Chiari 0 malformation. Neurosurgery 48:10501054, 2001

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 21

    Tubbs RS, , McGirt MJ, & Oakes WJ: Surgical experience in 130 pediatric patients with Chiari I malformations. J Neurosurg 99:291296, 2003

  • 22

    Tubbs RS, , Webb D, , Abdullatif H, , Conklin M, , Doyle S, & Oakes WJ: Posterior cranial fossa volume in patients with rickets: insights into the increased occurrence of Chiari I malformation in metabolic bone disease. Neurosurgery 55:380384, 2004

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 23

    Tubbs RS, , Wellons JC III, , Blount JP, & Oakes WJ: Syringomyelia in twin brothers discordant for Chiari I malformation: case report. J Child Neurol 19:459462, 2004

  • 24

    Tubbs RS, , Wellons JC III, , Smyth MD, , Bartolucci AA, , Blount JP, & Oakes WJ, et al.: Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa. Pediatr Neurosurg 38:324328, 2003

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 25

    Yabe I, , Kikuchi S, & Tashiro K: Familial syringomyelia: the first Japanese case and review of the literature. Clin Neurol Neurosurg 105:6971, 2002

  • 26

    Zakeri A, , Glasauer FE, & Egnatchik JG: Familial syringomyelia: case report and review of the literature. Surg Neurol 44:4853, 1995

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